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A Rare Coexistence of Retroperitoneal Pararenal Castlemans Disease with Focal Nodular Hyperplasia

机译:腹膜后肾旁Castleman病与局灶性结节性增生的罕见共存

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摘要

Castleman's disease is a distinct form of lymph node hyperplasia divided into a solitary and a multicentric type. The solitary type occurs most commonly in the mediastinum and is usually asymptomatic. We present a patient with Castleman's disease of the hyaline-vascular solitary type located in the retroperitoneum. The patient was a 38-year-old male, who presented to our hospital with fever. The imaging workup revealed a retroperitoneal mass, measuring 4 × 6 cm, located lateral to the aorta, inferior to the left renal artery and vein, and posterior to the left testicular vein. At workup, a solid hepatic lesion, 3 cm in diameter, located in the left lobe of the liver, segment IV, was also identified. Both lesions were surgically excised. The retroperitoneal tumor had the features of angiofollicular hyperplasia (Castleman's disease), hyaline-vascular type, whereas a diagnosis of focal nodular hyperplasia was made for the hepatic lesion. The patient is well at fourty months followup postoperatively. Surgical excision is the treatment of choice for unifocal Castleman's disease.
机译:Castleman病是淋巴结增生的一种独特形式,分为单发型和多中心型。孤独型最常见于纵隔,通常无症状。我们介绍了位于腹膜后的透明血管孤立型Castleman病患者。该患者是一名38岁的男性,因发烧到我们医院就诊。影像学检查显示腹膜后肿块,大小为4×6 cm,位于主动脉外侧,在左肾动脉和静脉下方,在左睾丸静脉之后。在检查时,还发现了位于肝脏左叶IV段的直径3 cm的实性肝病变。两种病变均通过手术切除。腹膜后肿瘤具有血管滤泡增生(卡斯尔曼病),透明血管型的特征,而肝病灶可诊断为局灶性结节性增生。术后四十个月随访情况良好。手术切除是治疗单灶性卡斯曼氏病的一种选择。

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